Fourier transform microwave spectroscop

The interaction of dihalogen molecules XY with different acceptors B quite often leads to vicious chemical reactions. In most cases, the 1 1 complexes are extremely short-lived. To investigate these prereactive complexes experimentally in a collision-free environment, pulsed-nozzle, Fourier-transform microwave spectroscopy has turned out to be the ideal technique. Legon and coworkers prepared a large number of these complexes and performed detailed rotational spectroscopic analyses. Several series of simple molecules... 

The preceding, somewhat historical, review of spectroscopic structural methods is more-or-less complete up to the 1980s. Of course, many new experimental tools had appeared by this time and were leading to additional high-quality data, often with unprecedented precision. These included Fourier-transform microwave spectroscopy... 

There have been extensive experimental and theoretical studies devoted to the structural and bonding characterization of weakly bound van der Waals complexes of acetylene. Structures of these complexes can often be determinated experimentally by means of Fourier transform microwave and infrared spectroscopic techniques. On the theoretical side, advanced treatments are required to understand the complex nature of the weak bonding in terms of the relative contributions of polarization and dispersion interactions, interactions of multiple moments, and electrostatic interactions involved in these completes. To determine the interaction energy in a weak complex, it is necessary to use large basis sets with the inclusion of electron correlation interactions. Theoretical calculations have been reported for van der Waals complexes of acetylene with COj [160], CO [161, 162], AICI3 [163], NH3 [164], He [165], Ar [166], H2O [167], HCN [168], HF [169-172], HCl [173, 174], and acetylene itself in the forms of non-covalent dimer [175-180], trimer [175,181], tetramer [175, 182, 183], and pentamer [175]. These calculations are very useful for the determination of multiple isomeric forms of the complex. For example, calculations at the MP2/6-31G level along with IR spectra indicate that the HCN-acetylene complex exists in a linear form in addition to the T-shaped structure observed previously by microwave studies (see Fig. 1-5) [168]. 

Similar to 2DR, ribose (C5H5O5) is one of the most important monosaccharides since it constitutes a subunit of the backbone of RNA. NMR studies have shown that ribose in solution is a mixture of a- and p-pyranose and a- and p-furanose forms, the p-pyranose form being predominant. The recently settled crystal structures have shown that the a- and P-pyranose forms are present in the solid phase [239-243]. The structure in the gas phase has been experimentally investigated using a laser ablation molecular beam Fourier transform microwave spectroscopy (LA-MBFTMW) technique [62]. The high resolution rotational spectrum has provided structural information on a total of six rotamers of ribose, three belonging to the a-pyranose forms and other three to the P-pyranose forms. Recently, D-ribose (m.p. 95°C) has been submitted to a laser ablation broadband (CP-FTMW) spectroscopic study and eight conformers (two new a-pyranose forms) have been identified. A broadband section of the spectra is shown in Fig. 35 and the detected conformers depicted in Fig. 36. 

Fourier transform techniques are used throughout the whole spectroscopic region, particularly in the infrared and visible. As we pass from the microwave region to the far-infrared, Fourier transform methods are still used, but based now on interferometry rather than pulsed methods. Perhaps this region of the spectrum will, in... 

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